Dyschromatosis universalis hereditaria
A rare genetic pigmentation anomaly of the skin characterized by generalized irregularly shaped asymptomatic hyper- and hypopigmented macules distributed in a reticular pattern involving the trunk limbs and sometimes the face. The palms soles and mucosa are usually not affected. Systemic abnormalities have been rarely reported.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2024
Newly diagnosed with
Dyschromatosis universalis hereditaria?
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Advocacy Organizations
Syndromes Without A Name (SWAN) Australia
Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
Clinical Trials
For a list of clinical trials in this disease area, please click here.